Jobs · Quality Assurance · Texas

Quality Control Tech 1

Katalyst CRO · El Paso, TX · 1 mo ago
On-siteQuality AssuranceContract

Responsibilities

  • Maintain Quality Reports.
  • Maintain and implement efforts in housekeeping and safety programs.
  • Maintain the cleanliness and orderliness of the Metrology Laboratory.
  • Perform raw material sampling.
  • Perform raw material inspections (except for raw material chemicals).
  • Understand and consistently follow multi‑step documented procedures while conducting inspections.
  • Maintain accurate and well‑organized inspection records, notebooks, and/or worksheets.
  • Maintain the Calibration and Preventive Maintenance programs for equipment.
  • Provide QC support for new product development, launch, and capacity expansion projects.
  • Support waste‑reduction initiatives that involve incoming inspection.
  • Demonstrate regulatory compliance such as FDA inspection readiness, corporate audits, internal audits, and maintain training compliance.
  • Demonstrate safety compliance, striving for zero serious accidents in the plant.
  • Contribute to successful EH&S audits with zero major observations and help achieve an overall safety index plant goal of >98%.
  • Maintain awareness and respect of all company policies and safety rules.
  • Maintain appropriate training/certification including GLP and GMP.

Requirements

  • High School diploma.
  • Experience in Quality Control, Incoming Inspection, or Metrology Laboratory operations (preferred).
  • Strong understanding of GLP, GMP, and regulatory compliance requirements.
  • Ability to follow detailed, multi‑step procedures with a high level of accuracy and attention to detail.
  • Experience maintaining calibration and preventive maintenance records for laboratory or inspection equipment.
  • Strong organizational, documentation, and communication skills.
  • Demonstrated commitment to safety, quality, and continuous improvement.
  • 1–2 years’ experience reading drawings and using measuring tools such as calipers, rulers, and vision systems (preferred).
  • Conversant with GLP/GCP/cGMP and global drug and device development processes (preferred).

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